A Japanese familial ALS patient with autonomic failure and a p.Cys146Arg mutation in the gene for SOD1 (SOD1). Issue 6 (18th April 2016)

• Record Type: Journal Article
• Authors: Hayashi, Kentaro; Mochizuki, Yoko; Koide, Reiji; Kawata, Akihiro; Homma, Taku; Shimizu, Toshio; Komori, Takashi; Isozaki, Eiji
• Is Part Of: Neuropathology. Volume 36:Issue 6(2016:Dec.)
• Page Start: 551
• Page End: 555
• Publication Date: 2016-04-18
• Subjects: autonomic failure -- familial ALS -- orthostatic hypotension -- SOD1 -- p.Cys146Arg; Nervous system -- Diseases -- Periodicals; Nervous system -- Pathophysiology -- Periodicals; 616.8047
• DOI: 10.1111/neup.12303
• Languages: English
• ISSNs: 0919-6544

Abstract

Abstract : We describe a Japanese man with familial amyotrophic lateral sclerosis (ALS) associated with a p.Cys146Arg mutation in the copper/zinc superoxide dismutase gene ( SOD1 ). The patient developed bulbar signs followed by rapidly progressive limb muscle weakness. The prominent clinical feature was orthostatic hypotension due to autonomic failure, which occurred after he underwent tracheostomy 1 year and 3 months after the onset. Thereafter, he required mechanical ventilation and progressed to communication stage V (totally locked‐in state) 7 years after the onset. Neuropathology showed ALS with posterior column degeneration and multiple system degeneration. Severe neuronal loss in the intermediolateral nucleus was also observed. Two previously reported cases of ALS patients with autonomic failure showed severe neuronal loss in the intermediolateral nucleus in addition to degeneration of the motor neurons. Thus, autonomic failure due to neuronal loss in the intermediolateral nucleus could present in patients with ALS associated with certain mutations in SOD1 .